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Progress in the chemistry of organic natural products [Vol. 119] (Record no. 566471)

MARC details
000 -LEADER
fixed length control field 02140 a2200361 4500
003 - CONTROL NUMBER IDENTIFIER
control field OSt
005 - DATE AND TIME OF LATEST TRANSACTION
control field 20230306125112.0
008 - FIXED-LENGTH DATA ELEMENTS--GENERAL INFORMATION
fixed length control field 230303b xxu||||| |||| 00| 0 eng d
020 ## - INTERNATIONAL STANDARD BOOK NUMBER
ISBN 9783031104565
040 ## - CATALOGING SOURCE
Transcribing agency IIT Kanpur
041 ## - LANGUAGE CODE
Language code of text/sound track or separate title eng
082 ## - DEWEY DECIMAL CLASSIFICATION NUMBER
Classification number 547
Item number P943 v.119
245 ## - TITLE STATEMENT
Title Progress in the chemistry of organic natural products [Vol. 119]
Remainder of title ancistrocladus naphthylisoquinoline alkaloids
Statement of responsibility, etc edited by A. Douglas Kinghorn ... [et al.]; Doris Feineis and Gerhard Bringmann
260 ## - PUBLICATION, DISTRIBUTION, ETC. (IMPRINT)
Name of publisher Springer
Year of publication 2023
Place of publication Switzerland
300 ## - PHYSICAL DESCRIPTION
Number of Pages xi, 335p
440 ## - SERIES STATEMENT/ADDED ENTRY--TITLE
Title Progress in the chemistry of organic natural products
490 ## - SERIES STATEMENT
Series statement / edited by A. Douglas Kinghorn... [et al.]
Volume number/sequential designation v.119
520 ## - SUMMARY, ETC.
Summary, etc This book describes a unique class of secondary metabolites, the mono- and dimeric-naphthylisoquinoline alkaloids. They exclusively occur in lianas of the palaeotropical Ancistrocladaceae and Dioncophyllaceae plant families. Their unprecedented structures include stereogenic centers and rotationally hindered, and therefore stereogenic, axes. Extended recent investigations on six Ancistrocladus species from Asia, as reported in this contribution, shed light on their fascinating phytochemical productivity, with over 100 intriguing natural products. This high chemodiversity arises from a similarly unique biosynthesis from acetate-malonate units, following a novel polyketidic pathway to plant-derived isoquinoline alkaloids. Some of the compounds show most promising anti-parasitic activities. Additionally, strategies for the regio- and stereoselective total synthesis of the alkaloids, including the directed construction of the chiral axis, are also presented.
650 ## - SUBJECT ADDED ENTRY--TOPICAL TERM
Topical Term Natural products
650 ## - SUBJECT ADDED ENTRY--TOPICAL TERM
Topical Term Chemistry, Organic
650 ## - SUBJECT ADDED ENTRY--TOPICAL TERM
Topical Term Ancistrocladus
650 ## - SUBJECT ADDED ENTRY--TOPICAL TERM
Topical Term Naphthylisoquinoline
650 ## - SUBJECT ADDED ENTRY--TOPICAL TERM
Topical Term Alkaloids
700 ## - ADDED ENTRY--PERSONAL NAME
Personal name Kinghorn, A. Douglas [ed.]
700 ## - ADDED ENTRY--PERSONAL NAME
Personal name Falk, Heinz [ed.]
700 ## - ADDED ENTRY--PERSONAL NAME
Personal name Gibbons, Simon [ed.]
700 ## - ADDED ENTRY--PERSONAL NAME
Personal name Asakawa, Yoshinori [ed.]
700 ## - ADDED ENTRY--PERSONAL NAME
Personal name Liu, Ji-Kai [ed.]
700 ## - ADDED ENTRY--PERSONAL NAME
Personal name Dirsch, Verena M. [ed.]
700 ## - ADDED ENTRY--PERSONAL NAME
Personal name Feineis, Doris
700 ## - ADDED ENTRY--PERSONAL NAME
Personal name Bringmann,Gerhard
942 ## - ADDED ENTRY ELEMENTS (KOHA)
Koha item type Books
Holdings
Withdrawn status Lost status Damaged status Not for loan Collection code Home library Current library Date acquired Source of acquisition Cost, normal purchase price Full call number Accession Number Cost, replacement price Koha item type
        General Stacks PK Kelkar Library, IIT Kanpur PK Kelkar Library, IIT Kanpur 20/03/2023 12 11315.77 547 P943 v.119 A186073 14144.72 Books

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